According to the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guideline Q2(R1), specificity is…
UV development can refer to several distinct areas, primarily revolving around ultraviolet (UV) light and its applications. To provide a…
Ah, method validation planning in pharma – a cornerstone of ensuring the quality and reliability of pharmaceutical products! It's all…
heavy metals in a substance. It involves reacting the substance with hydrogen sulfide (or sodium sulfide) to produce colored heavy…
measures the fluorescence emitted by atoms in a sample excited by a light source. X-ray Absorption Spectroscopy (XAS): XAS provides…
HPLC (High-Performance Liquid Chromatography) method development is a critical process in analytical chemistry, involving the creation of a precise and…
Type of analytical procedure validated Identification tests. Quantitative tests for impurities' content. Limit tests for the control of impurities. Quantitative…
In HPLC chromatography, the column is where the separation of the sample takes place. This is where the sample is…
HPLC Analyst ○ Whenever supervisor give work allocation for testing any product. ○ HPLC analyst first seen Test which is…